Abstract:ObjectiveTo evaluate the blocking effect and mechanism of Soybeanderived BowmanBirk inhibitor (BBI) on LPSmediated downregulation for tight junction protein(HT29 cells) in intestinal epithelial cells(IECs).MethodsThe toxic effect of LPS and BBI on HT29 cells was detected by CCK8 Kit. HT29 cells were pretreated by BBI for 6 hours prior to LPS stimulation, the expression of tight junction protein (ZO1 and Occludin), TLR4, and MyDD8 was detected by the quantitative realtime polymerase chain reaction (PCR) and Western Blot; activation of NFκB was measured by Western Blot.ResultsLPS (1 000ng/mL) and BBI (1 000μg/mL) showed no cytotoxicity on HT29 cells. LPS could significantly upregulate the expression of TLR4 in HT29 cells, the upregulation had timedose effect, and could significantly downregulate the expression of tight junction protein, the downregulation effect was directly proportional to the concentration of LPS, could activate NFκB, and had dose effect, effect of LPS on HT29 cells could be significantly inhibited by BBI.ConclusionBy inhibiting the expression of TLR4 and activation of NFκB in IECs induced by LPS, BBI can significantly block the LPSmediated inhibitory effect on tight junction protein in intestinal epithelial cells.